Brain-based gene expression and corresponding behavioural relevance of risk genes for broad antisocial behaviour

IF 4.7 2区 医学 Q1 NEUROIMAGING
Jaroslav Rokicki , Megan L. Campbell , Dennis van der Meer , Alina I. Sartorius , Natalia Tesli , Piotr Jahołkowski , Alexey Shadrin , Ole Andreassen , Lars T. Westlye , Daniel S. Quintana , Unn K. Haukvik
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引用次数: 0

Abstract

Antisocial behaviour (ASB) involves persistent irresponsible, delinquent activities violating rights and safety of others. A meta-analysis of genome-wide association studies revealed significant genetic associations with ASB, yet their brain expression patterns and behavioural relevance remain unclear. Our investigation of fifteen genes associated with ASB examined their biological role and distribution across tissues, integrating post-mortem brain sample data from the Allen-Human-Brain Atlas and the Genotype-Tissue Expression project. We found that these genes were differentially expressed in the brain, particularly in regions like the cerebellum, putamen, and caudate, and were notably downregulated in the pancreas. Single cell type expression analysis revealed that ASB-associated genes had strong correlations with ductal and endothelial cells in the pancreas, indicating a possible metabolic influence on ASB. Certain genes like NTN1, SMAD5, NCAM2, and CDC42EP3 displayed specificity for cognitive terms including chronic pain, heart rate, and aphasia. These expression patterns aligned with neurocognitive domains related to thinking, and learning, distress, motor skills, as determined by fMRI analysis. This study connects specific brain gene expression with potential genetic and metabolic factors in ASB, offering novel insights into its biological basis and possible interdisciplinary approaches to understanding and addressing aggressive behaviours.
基于大脑的基因表达和相应的反社会行为风险基因的行为相关性
反社会行为(ASB)包括持续的侵犯他人权利和安全的不负责任的违法行为。一项全基因组关联研究的荟萃分析显示,自闭症与ASB存在显著的遗传关联,但其大脑表达模式和行为相关性尚不清楚。我们对15个与ASB相关的基因进行了研究,研究了它们在组织中的生物学作用和分布,并整合了来自Allen-Human-Brain Atlas和基因型组织表达项目的死后脑样本数据。我们发现这些基因在大脑中有差异表达,特别是在小脑、壳核和尾状核等区域,在胰腺中明显下调。单细胞类型表达分析显示,ASB相关基因与胰腺导管细胞和内皮细胞有很强的相关性,表明可能存在代谢对ASB的影响。某些基因如NTN1、SMAD5、NCAM2和CDC42EP3在认知方面表现出特异性,包括慢性疼痛、心率和失语。这些表达模式与与思考、学习、痛苦、运动技能相关的神经认知领域一致,这是由功能磁共振成像分析确定的。本研究将ASB中特定的大脑基因表达与潜在的遗传和代谢因素联系起来,为其生物学基础提供了新的见解,并为理解和解决攻击行为提供了可能的跨学科方法。
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来源期刊
NeuroImage
NeuroImage 医学-核医学
CiteScore
11.30
自引率
10.50%
发文量
809
审稿时长
63 days
期刊介绍: NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.
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